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VERSION:2.0
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CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20240329T083207Z
UID:8210238a-088f-4c5a-afe8-25d6016aa755
DTSTART:20210204T100000
DTEND:20210205T100000
CLASS:PRIVATE
DESCRIPTION:Overview:
\nYou'\;ll learn about the various computer s
ystem validation deliverables and how to document them through the entire
process. You will learn about what must be done to ensure the system remai
ns in a validated state.
\n
\nWhy should you Attend:
\nThis
webinar will help you understand in detail Computer System Validation (CS
V) and how to apply the System Development Life Cycle (SDLC) Methodology w
hen validating computer systems subject to FDA regulations.
\n
\
nAreas Covered in the Session:
\nInstallation Qualification
\nOp
erational Qualification
\nPerformance Qualification
\nPolicies a
nd Procedures
\nTraining
\nOrganizational Change Management
\n
\nWho Will Benefit:
\nClinical Data Managers and Scientists<
br />\nCompliance Managers and Auditors
\nLab Managers and Analysts\nComputer System Validation Specialists
\nGMP Training Specialis
ts
\n
\nSpeaker Profile:
\nCarolyn (McKillop) Troiano has m
ore than 35 years of experience in the tobacco\, pharmaceutical\, medical
device and other FDA-regulated industries. She has worked directly\, or on
a consulting basis\, for many of the larger pharmaceutical and tobacco co
mpanies in the US and Europe\, developing and executing compliance strateg
ies and programs.
\n
\nEvent Fee: One Dial-in One Attendee Price
: US$150.00
\n
\nContact Detail:
\nCompliance4All DBA NetZe
alous\,
\nPhone: +1-800-447-9407
\nEmail: support@compliance4All
.com
SUMMARY:How to Validate for Regulated Computer Systems
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SUMMARY:How to Validate for Regulated Computer Systems
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